Literature DB >> 7681431

Axial filament formation in Bacillus subtilis: induction of nucleoids of increasing length after addition of chloramphenicol to exponential-phase cultures approaching stationary phase.

J E Bylund1, M A Haines, P J Piggot, M L Higgins.   

Abstract

When chloramphenicol was added to a culture of Bacillus subtilis in early exponential growth, microscopic observation of cells stained by 4',6-diamidino-2-phenylindole showed nucleoids that had changed in appearance from irregular spheres and dumbbells to large, brightly stained spheres and ovals. In contrast, the addition of chloramphenicol to cultures in mid- and late exponential growth showed cells with elongated nucleoids whose frequency and length increased as the culture approached stationary phase. The kinetics of nucleoid elongation after the addition of chloramphenicol to exponential-phase cultures was complex. Immediately after treatment, the rate of nucleoid elongation was very rapid. The nucleoid then elongated steadily for about 4 min, after which the rate of elongation decreased considerably. Nucleoids of cells treated with 6-(p-hydroxyphenylazo)-uracil (an inhibitor of DNA synthesis) exhibited the immediate rapid elongation upon chloramphenicol treatment but not the subsequent changes. These observations suggest that axial filament formation during stationary phase (stage I of sporulation) in the absence of chloramphenicol results from changes in nucleoid structure that are initiated earlier, during exponential growth.

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Year:  1993        PMID: 7681431      PMCID: PMC204252          DOI: 10.1128/jb.175.7.1886-1890.1993

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  23 in total

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Journal:  J Bacteriol       Date:  1961-04       Impact factor: 3.490

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Review 4.  Functional consequences of improved structural information on bacterial nucleoids.

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7.  Electron microscopy of chloramphenicol-treated Escherichia coli.

Authors:  C Morgan; H S Rosenkranz; H S Carr; H M Rose
Journal:  J Bacteriol       Date:  1967-06       Impact factor: 3.490

8.  Inhibition of bacterial DNA replication by 6-(p-hydroxyphenylazo)-uracil: differential effect on repair and semi-conservative synthesis in Bacillus subtilis.

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Journal:  J Mol Biol       Date:  1971-07-14       Impact factor: 5.469

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Journal:  Res Microbiol       Date:  1991 Feb-Apr       Impact factor: 3.992

10.  Electron microscope study of DNA-containing plasms. II. Vegetative and mature phage DNA as compared with normal bacterial nucleoids in different physiological states.

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Journal:  J Biophys Biochem Cytol       Date:  1958-11-25
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  16 in total

1.  A large dispersed chromosomal region required for chromosome segregation in sporulating cells of Bacillus subtilis.

Authors:  Ling Juan Wu; Jeff Errington
Journal:  EMBO J       Date:  2002-08-01       Impact factor: 11.598

Review 2.  Compartmentalization of gene expression during Bacillus subtilis spore formation.

Authors:  David W Hilbert; Patrick J Piggot
Journal:  Microbiol Mol Biol Rev       Date:  2004-06       Impact factor: 11.056

Review 3.  Diversity and redundancy in bacterial chromosome segregation mechanisms.

Authors:  Jeff Errington; Heath Murray; Ling Juan Wu
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2005-03-29       Impact factor: 6.237

4.  Shaping an Endospore: Architectural Transformations During Bacillus subtilis Sporulation.

Authors:  Kanika Khanna; Javier Lopez-Garrido; Kit Pogliano
Journal:  Annu Rev Microbiol       Date:  2020-07-13       Impact factor: 15.500

5.  Postseptational chromosome partitioning in bacteria.

Authors:  M E Sharpe; J Errington
Journal:  Proc Natl Acad Sci U S A       Date:  1995-09-12       Impact factor: 11.205

6.  Growth phase variation in cell and nucleoid morphology in a Bacillus subtilis recA mutant.

Authors:  S A Sciochetti; G W Blakely; P J Piggot
Journal:  J Bacteriol       Date:  2001-05       Impact factor: 3.490

7.  Postdivisional synthesis of the Sporosarcina ureae DNA translocase SpoIIIE either in the mother cell or in the prespore enables Bacillus subtilis to translocate DNA from the mother cell to the prespore.

Authors:  Vasant K Chary; Patrick J Piggot
Journal:  J Bacteriol       Date:  2003-02       Impact factor: 3.490

8.  Characterization of cell cycle events during the onset of sporulation in Bacillus subtilis.

Authors:  P M Hauser; J Errington
Journal:  J Bacteriol       Date:  1995-07       Impact factor: 3.490

9.  Bex, the Bacillus subtilis homolog of the essential Escherichia coli GTPase Era, is required for normal cell division and spore formation.

Authors:  Natalie Minkovsky; Arash Zarimani; Vasant K Chary; Brian H Johnstone; Bradford S Powell; Pamela D Torrance; Donald L Court; Robert W Simons; Patrick J Piggot
Journal:  J Bacteriol       Date:  2002-11       Impact factor: 3.490

10.  Characterization of divIVA and other genes located in the chromosomal region downstream of the dcw cluster in Streptococcus pneumoniae.

Authors:  Daniela Fadda; Carla Pischedda; Fabrizio Caldara; Michael B Whalen; Daniela Anderluzzi; Enrico Domenici; Orietta Massidda
Journal:  J Bacteriol       Date:  2003-10       Impact factor: 3.490

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